|
Brugada Syndrome 1 (Sudden Unexplained Nocturnal Death Syndrome (SUNDS)) |
approved
|
601144 |
|
|
|
|
Calpainopathy |
approved
|
253600 |
|
|
Campomelic Dysplasia |
approved
|
114290 |
|
|
|
|
Canavan Disease |
approved
|
271900 |
|
|
Capillary Malformation-Arteriovenous Malformation Type 1 (CM-AVM1) |
approved
|
608354 |
|
|
|
|
Capillary Malformation-Arteriovenous Malformation Type 2 (CM-AVM2) |
approved
|
618196 |
|
|
|
|
Carney Complex |
approved
|
160980 |
|
|
Carnitine Acylcarnitine Translocase Deficiency (CACT) |
approved
|
212138 |
|
|
Cartilage-Hair Hypoplasia |
approved
|
250250 |
|
|
|
|
Cartilage-hair hypoplasia spectrum |
approved
|
157660 |
|
|
|
|
Cataract 1 (CTRCT1) |
approved
|
116200 |
|
|
|
|
Cataract 2 (CTRCT2) |
approved
|
604307 |
|
|
|
|
Cataract 4 (CTRCT4) |
approved
|
115700 |
|
|
|
|
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT1) |
approved
|
604772 |
|
|
Catecholaminergic Polymorphic Ventricular Tachycardia type 3 (CPVT3) |
approved
|
614021 |
|
|
|
|
Catecholaminergic Polymorphic Ventricular Tachycardia type 4 (CPVT4) |
approved
|
614916 |
|
|
|
|
Catecholaminergic Polymorphic Ventricular Tachycardia type 5 with or without muscle weakness (CPVT5) |
approved
|
615441 |
|
|
|
|
Catecholaminergic Polymorphic Ventricular Tachychardia 2 (CPVT2) |
approved
|
611938 |
|
|
Central Core Disease of Muscle (CCD) |
approved
|
117000 |
|
|
Centronuclear Myopathy (CNM1) |
approved
|
160150 |
|
|
|
